| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CEP72, LOC126807283 (L30R) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126807283, CEP72 (R63H) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene